Over-the-counter drug · ANDA

Minoxidil (For Men) (Minoxidil) NDC 85524-2611

Minoxidil 5 g/100g · Liquid · Topical · FlexiGo Inc

NDC codes

FDA NDC Directory
Product NDC (as listed)85524-2611Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85524-2611Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
85524-2611-285524261102855242611023 BOTTLE in 1 BAG (85524-2611-2) / 60 g in 1 BOTTLE (85524-2611-1)Marketed from Jun 8, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Minoxidil (For Men)
Generic name (nonproprietary)
minoxidil
Active ingredients
Minoxidil — 5 g/100g
Dosage form
Liquid
Route
Topical
Labeler
FlexiGo IncNDC labeler code 85524
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218616
Marketing start
Listing expires
Other FDA classes
Arteriolar Vasodilation (Physiologic effect)
Identifiers
Product ID 85524-2611_53793182-8a04-1b0f-e063-6294a90acca6SPL ID 53793182-8a04-1b0f-e063-6294a90acca6SPL set ID 53793182-8a03-1b0f-e063-6294a90acca6RxCUI 645146UNII 5965120SH1
Pharmacologic class
Arteriolar Vasodilator

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N485524261102 followed by a unit qualifier and the quantity

Package 85524-2611-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85524-2611

What is NDC 85524-2611?
85524-2611 is the product NDC for Minoxidil (For Men) (minoxidil), Minoxidil 5 g/100g liquid, listed with the FDA by FlexiGo Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Minoxidil (For Men) (Minoxidil).
What is the active ingredient?
Minoxidil.
Who is the labeler?
FlexiGo Inc, NDC labeler code 85524. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Minoxidil (For Men)?
8 other product NDCs are listed under this name. See all Minoxidil (For Men) NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Minoxidil (For Men) NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Minoxidil For MenminoxidilMinoxidil 50 mg/gAerosol, FoamTopicalCARDINAL HEALTH 110, LLC. DBA LEADER70000-075470000-0754-01
Minoxidil For MenminoxidilMinoxidil 50 mg/gAerosol, FoamTopicalBosleyMD69113-50169113-0501-01
Minoxidil (for Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalRESTORATION HOLDINGS, LLC82796-10082796-0100-01
Minoxidil (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalSPAZI INC.82376-600682376-6006-03
Minoxidil (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalWalgreen Company0363-909000363-9090-0100363-9090-03
Minoxidil (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalCVS Pharmacy51316-21251316-0212-0351316-0212-1051316-0212-30
Minoxidil (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalTARGET Corporation11673-15711673-0157-0311673-0157-09
Minoxidil (for Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalSCIENTIFIC HAIR RESEARCH, LLC69113-12869113-0128-0169113-0128-03

Other NDCs under ANDA 218616

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 218616
ProductStrengthForm · routeLabelerProduct NDC
Minoxidil 5% (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalBetter Living Brands, LLC21130-208
Minoxidil 5% (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalAurohealth LLC58602-608
Minoxidil 5% (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalAurohealth LLC58602-614
Minoxidil 5% (For Women)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalAurohealth LLC58602-104
Minoxidil 5% (For Women)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalAurohealth LLC58602-607
Minoxidil For MenminoxidilMinoxidil 50 mg/gAerosol, FoamTopicalCARDINAL HEALTH 110, LLC. DBA LEADER70000-0754
Minoxidil For WomenminoxidilMinoxidil 50 mg/gAerosol, FoamTopicalCARDINAL HEALTH 110, LLC. DBA LEADER70000-0753
Nizoral Hair Regrowth Treatment for MenminoxidilMinoxidil 50 mg/gAerosol, FoamTopicalKramer Laboratories55505-237
Regoxidine (For Men)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalINNOVUS PHARMACEUTICALS, INC.57483-165
Regoxidine (For Women)minoxidilMinoxidil 50 mg/gAerosol, FoamTopicalINNOVUS PHARMACEUTICALS, INC.57483-175

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